A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153434



Internal ID20720474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130398935..130399635hg38UCSC Ensembl
chr7:130038776..130039476hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431872
Supporting Variants
Samples
Known GenesCEP41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer